US10078215B2 - Shutter assembly for a luminescence-based sample analyzer - Google Patents

Shutter assembly for a luminescence-based sample analyzer Download PDF

Info

Publication number
US10078215B2
US10078215B2 US15/691,842 US201715691842A US10078215B2 US 10078215 B2 US10078215 B2 US 10078215B2 US 201715691842 A US201715691842 A US 201715691842A US 10078215 B2 US10078215 B2 US 10078215B2
Authority
US
United States
Prior art keywords
shutter
light transmitting
shutter assembly
aperture
apertures
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
US15/691,842
Other versions
US20180045950A1 (en
Inventor
Jeffrey R. Jasperse
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Siemens Healthcare Diagnostics Inc
Original Assignee
Siemens Healthcare Diagnostics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Siemens Healthcare Diagnostics Inc filed Critical Siemens Healthcare Diagnostics Inc
Priority to US15/691,842 priority Critical patent/US10078215B2/en
Assigned to SIEMENS HEALTHCARE DIAGNOSTICS INC. reassignment SIEMENS HEALTHCARE DIAGNOSTICS INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JASPERSE, JEFFREY R.
Publication of US20180045950A1 publication Critical patent/US20180045950A1/en
Application granted granted Critical
Publication of US10078215B2 publication Critical patent/US10078215B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B26/00Optical devices or arrangements for the control of light using movable or deformable optical elements
    • G02B26/02Optical devices or arrangements for the control of light using movable or deformable optical elements for controlling the intensity of light
    • G02B26/04Optical devices or arrangements for the control of light using movable or deformable optical elements for controlling the intensity of light by periodically varying the intensity of light, e.g. using choppers
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/543Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J43/00Secondary-emission tubes; Electron-multiplier tubes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/02Mechanical
    • G01N2201/022Casings
    • G01N2201/0221Portable; cableless; compact; hand-held
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/06Illumination; Optics
    • G01N2201/064Stray light conditioning
    • G01N2201/0648Shutters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/06Illumination; Optics
    • G01N2201/068Optics, miscellaneous
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03BAPPARATUS OR ARRANGEMENTS FOR TAKING PHOTOGRAPHS OR FOR PROJECTING OR VIEWING THEM; APPARATUS OR ARRANGEMENTS EMPLOYING ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ACCESSORIES THEREFOR
    • G03B11/00Filters or other obturators specially adapted for photographic purposes
    • G03B11/04Hoods or caps for eliminating unwanted light from lenses, viewfinders or focusing aids
    • G03B11/043Protective lens closures or lens caps built into cameras
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03BAPPARATUS OR ARRANGEMENTS FOR TAKING PHOTOGRAPHS OR FOR PROJECTING OR VIEWING THEM; APPARATUS OR ARRANGEMENTS EMPLOYING ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ACCESSORIES THEREFOR
    • G03B9/00Exposure-making shutters; Diaphragms
    • G03B9/08Shutters
    • G03B9/10Blade or disc rotating or pivoting about axis normal to its plane
    • G03B9/14Two separate members moving in opposite directions

Definitions

  • inventive concepts disclosed and claimed herein relate generally to shutters, and more particularly, but not by way of limitation, to a shutter assembly for protecting a sensitive light detector such as a photomultiplier tube against harmful exposure to light.
  • Analytical instrumentation utilizing luminescence detection is heavily utilized in the pharmaceutical and medical industries. Analytical measurements are often performed using a beam of catalyzing radiation to interact with a specific sample-reagent combination. The resulting photon emission, often very weak, is then detected and measured with a sensitive detector, converted to an electrical signal, and further correlated to provide the actual analytical result.
  • U.S. Pat. No. 5,709,994 discloses a highly sensitive method of assaying known as a Luminescent Oxygen Channeling Immunoassay (LOCI).
  • LOCI Luminescent Oxygen Channeling Immunoassay
  • the method uses a photosensitizer that generates singlet oxygen upon irradiation, and a chemiluminescent compound that is activated by the singlet oxygen.
  • the photosensitizer and chemiluminescent compound are irradiated with light of a certain wavelength, after which the resulting light emitted by chemiluminescent compound is measured and correlated to provide the assay.
  • the instrumentation utilized for luminescence-based assays is often physically large due, in part, to the intricate and sensitive optics used.
  • the analyses often involve exposure of the sample to a high intensity light near the field of view of a sensitive detector such as a photomultiplier tube.
  • a sensitive detector such as a photomultiplier tube.
  • it is common to widely separate the detector from the high intensity light source and to provide path barriers and shutters between the two.
  • the inventive concepts disclosed and claimed herein generally relate to a shutter assembly for interrupting light transmission.
  • the shutter assembly includes a first shutter blade having a first toothed arm extending therefrom and a first light transmitting aperture therein, and a second shutter blade positioned adjacent and parallel to the first shutter blade.
  • the second shutter blade has a second toothed arm extending therefrom and a second light transmitting aperture therein.
  • the first and second shutter blades are supported to allow parallel linear motion.
  • a motor gear is disposed between, and meshed with, the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another.
  • FIG. 1 is a schematic representation of an embodiment of a sample analyzer constructed in accordance with the inventive concepts disclosed herein.
  • FIG. 2 is a schematic representation of an embodiment of a shutter assembly constructed in accordance with the inventive concepts disclosed herein.
  • FIG. 3 is a timing diagram for an embodiment of a sample analyzer operation in accordance with the inventive concepts disclosed herein.
  • FIG. 4A - FIG. 4F provide a schematic representation of a shutter assembly embodiment operating in accordance with the inventive concepts disclosed herein.
  • FIG. 5A - FIG. 5F provide a schematic representation of another shutter assembly embodiment operating in accordance with the inventive concepts disclosed herein.
  • FIG. 6A - FIG. 6C provide a schematic representation of yet another shutter assembly embodiment showing use and placement of reference aperture sensors.
  • inventive concept is not limited in its application to the details of construction, experiments, exemplary data, and/or the arrangement of the components set forth in the following description, or illustrated in the drawings.
  • inventive concept is capable of other embodiments or of being practiced or carried out in various ways.
  • phraseology and terminology employed herein is for purpose of description only and should not be regarded as limiting in any way.
  • references to the Luminescent Oxygen Channeling Immunoassay (LOCI) methods and optical systems are for example only, and the inventive concepts can be used with any sample analysis procedure utilizing optical detection to measure luminescence, fluorescence, absorbance, and turbidity.
  • Reference to a “sample” or “assay sample” refers to the sample to be analyzed and includes reagents added according to the analysis procedure, those reagents added either before or after insertion into the assay sample vessel.
  • any reference to “one embodiment” or “an embodiment” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment.
  • the appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
  • the sample analyzer 10 comprises an illuminator 12 for illuminating an assay sample 14 positioned and contained within a sample reservoir 16 to cause luminescence.
  • a shutter assembly 18 is positioned along an optical axis 20 to protect the sensitive optics of detector 22 from high intensity illumination from the illuminator 12 .
  • the detector 22 measures the luminescence or light emitted from assay sample 14 as a result of the illumination.
  • the illuminator 12 can be multi-wavelength, optionally filtered to cut off undesired wavelengths, or can be a laser providing monochromatic light. Light intensity and time of irradiation may vary widely. In one embodiment, light emitting diodes (LEDs) are used. In another embodiment, the illuminator 12 comprises multiple LEDs arranged in a ring.
  • LEDs light emitting diodes
  • the detector 22 can be any known or yet to be developed photo-detector having a sensitivity required by the particular assay.
  • vacuum photodetectors such as photomultiplier tubes (PMTs) are typically very sensitive compared to solid state photodetectors such as silicon photodiodes. Photodetectors and their use are well known to those skilled in the art.
  • Optical axis 20 is defined herein by a line directed from the illuminator 12 to the detector 22 . In some embodiments, and as shown in FIG. 1 , optical axis 20 also coincides with a line directed from the positioned sample reservoir 16 to the detector 22 . Such alignment of the illuminator 12 with both the sample reservoir 16 and the detector 22 provides a shortened optical path for both illumination and measuring modes. This in turn allows a more compact design and reduced power requirements compared to existing laboratory luminescence-based sample analyzers. For example, in one embodiment, the detector 22 is positioned about 10 mm or less from the assay sample 14 . In another embodiment, the detector 22 is positioned about 5 mm or less from the assay sample 14 .
  • the distance between the detector and the assay sample is on the order of 80 mm or more.
  • the detector 22 is positioned about 5 mm from the illuminator 12 . This is a significant achievement, particularly in embodiments utilizing a photomultiplier tube to measure extraordinarily low light signals of interest on the order of 50 photons per second output.
  • Such compaction provides embodiments wherein the sample analyzer 10 is portable and/or hand-held and the power supply 24 is one or more batteries.
  • the shutter assembly 18 operates to remain closed during the illumination interval, thereby blocking light transmission from the illuminator 12 to the detector 22 and protecting the detector 22 from over exposure.
  • light shines into the assay sample reservoir 16 , activating the assay sample 14 to start the reaction and photon emission.
  • the shutter assembly 18 remains open to allow light emitted by the assay sample to enter and be measured by detector 22 .
  • This unique design enables the use of rigid, dense blade material, such as metal alloys, achieving the highest degree of optical density performance possible while providing high speed shutter opening and closing, a critical need in high intensity illumination applications that use a high sensitivity photon detector.
  • a surface 25 of the shutter assembly 18 facing the illuminator 12 is reflective, such that light from the illuminator 12 passing through the assay sample 14 is reflected by the surface 25 back toward the assay sample 14 . This increases the illumination penetrating the assay sample 14 and thereby improves the assay sample activation.
  • a nonlimiting example of a suitable reflective surface 25 is polished stainless steel.
  • the shutter assembly 18 comprises a first shutter blade 26 and a second shutter blade 28 .
  • First shutter blade 26 is planar in shape with a first toothed arm 30 extending therefrom and a first light transmitting aperture 32 therein.
  • the second shutter blade 28 is planar in shape with a second toothed arm 34 extending therefrom and a second light transmitting aperture 36 therein.
  • the second shutter blade 28 is positioned adjacent and parallel to the first shutter blade 26 , and both shutter blades 26 and 28 are slideably supported on shutter assembly 18 to allow parallel linear motion.
  • First and second shutter blades 26 and 28 are typically shaped as thin metal blades with dimensions determined, in large part, by the sizes of the sample reservoir 16 and detector 22 .
  • Suitable construction can include any rigid material that is impervious to light.
  • suitable metal alloys and polymers are known to those skilled in the art and are readily available commercially.
  • the first and second shutter blades 26 and 28 were constructed of 0.127 mm thick 304 stainless steel. This material is readily available and provided a high degree of light blocking. The blades were treated with a black oxide coating to prevent photon tunneling and reflections. The friction caused between the blades was low, thereby providing a low torque requirement and allowing high speed operation.
  • the reflective surface 25 can be present on at least a portion of the first or second shutter blades 26 and 28 , wherein that portion represents the shutter blade surface exposed to illumination penetrating through the assay sample 14 during the illumination interval. It has been found that when first and second shutter blades 26 and 28 are constructed of stainless steel, polishing a portion of the stainless steel to produce the reflective surface 25 is sufficient to increase the illumination penetrating the assay sample 14 and to improve the assay sample activation.
  • First shutter blade 26 can include a lower arm 54 which does not require teeth as do first and second toothed arms 30 and 34 .
  • the shutter assembly 18 is operated by an actuator mechanism to cause the first and second shutter blades 26 and 28 , respectively, to move linearly in opposite directions between an open position in which the first and second light transmitting apertures 32 and 36 are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures 32 and 36 are in a non-overlapping relationship with respect to one another.
  • a suitable shutter actuator mechanism include a motor and solenoid with linkage to the shutter working against a spring, and a stepper motor.
  • a spring (not shown) or the like may be used to urge the first and second shutter blades 26 and 28 into a closed position to protect the detector 22 .
  • Shutters such as those used in cameras and laboratory instrumentation utilizing optical detection, such as luminescence, fluorescence, absorbance measurements, are commonly controlled using a solenoid working against a spring.
  • the solenoid requires continued power input to work against the spring or the like to maintain the shutter in an open position.
  • the analytical instruments requiring shutters are usually powered by AC current, and the solenoid power requirements are not a major concern. Battery power drain is not significant with camera shutters because the shutter typically does not remain open for long periods. However, because of the relatively long time the shutter must remain open in luminescence-based sample analyzers, the power required for operation of a solenoid-controlled shutter in a battery-operated luminescence-based sample analyzer is significant.
  • a motor 38 attached to the shutter assembly 18 by, for example, mountings 40 a and 40 b , provides a gear 42 which is disposed between, and meshed with, the first and second toothed arms 30 and 34 , respectively.
  • Rotation of gear 42 causes the first and second shutter blades 26 and 28 , respectively, to move linearly in opposite directions between an open position in which the first and second light transmitting apertures 32 and 36 are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures 32 and 36 are in a non-overlapping relationship with respect to one another.
  • motor 38 is a stepper motor.
  • a stepper motor is a brushless, electric motor having a number of “toothed” electromagnets arranged around a central gear-shaped bar of iron, each electromagnet providing a “step.” A full rotation is thus divided into a number of individual steps, and the motor's position can be precisely controlled without requiring a feedback mechanism.
  • torque decreases. The maximum torque occurs when the motor is stationary, and this “holding torque” determines the ability of the motor to maintain a desired position under external load.
  • stepper motor 38 advantageously provides a holding torque which can be used to maintain the shutter blades in a precisely controlled position, whether closed, full open, or any position between. Because the stepper motor 38 requires no power to maintain a shutter position, it reduces the power requirements of a portable luminescence-based analyzer making such battery powered devices practical.
  • stepper motor 38 the time taken for stepper motor 38 to open first and second shutter blades 26 and 28 , respectively, is fast, due in part because the mass of the shutter blades and resulting inertia is small, and because the stepper motor 38 can be run at its highest velocity, sometimes called “high speed slewing.”
  • the shutter assembly 18 utilizing stepper motor 38 can be used to control the exposure time of the detector 22 in addition to protecting the detector 22 from light from the illuminator 12 .
  • FIG. 3 is an example timing diagram depicting a LOCI Troponin I assay.
  • FIG. 3 timing sequence detail First the assay sample is illuminated; Second the shutter is opened to expose the detector optics to the assay sample; Third the detector is logically enabled to collect photon emission; Fourth the detector collecting photon emission is logically disabled; Fifth the shutter is closed to occlude and protect the detector.
  • the Notional Assay Flux Production waveform represents the signal of interest, the output of the assay sample is proportional to the analyte concentration.
  • FIG. 4A the first and second shutter blades 26 and 28 are noted at stepper motor 38 position “0” coinciding with the first and second light transmitting apertures 32 and 36 , respectively, being fully aligned thereby providing a full effective aperture 44 and noted as “FULL OPEN.”
  • FIG. 4B through FIG. 4F show an example of the relative positions of the shutter blades and apertures as stepper motor gear 42 progresses in 2-step intervals. After 6 steps, FIG. 4D shows no overlap of the first and second light transmitting apertures 32 and 36 , respectively, and therefore no effective aperture 44 .
  • reference apertures are also provided in the shutter blades.
  • FIG. 4A through FIG. 4F show the relative positions of a pinhole reference aperture 46 in the first shutter blade 26 , and a larger reference aperture 48 in the second shutter blade 28 .
  • the pinhole reference aperture 46 has a diameter of about 0.5 mm or less.
  • the larger reference aperture 48 has a diameter less than 25 percent of the diameter of the first and second light transmitting apertures 32 and 36 .
  • the pinhole reference aperture 46 and the large reference aperture 48 are positioned on either side of the respective first or second light transmitting aperture 26 or 28 , such that they are at a maximum distance of separation in the full open position shown in FIG. 4A , and overlapping after 8 steps as shown in FIG.
  • the pinhole reference aperture positioned as in FIG. 4E , allows only small quantities of light into the detector 22 , and can be used to monitor alignment or the light intensity transmitted by illuminator 12 for example.
  • FIG. 4F no light may be transmitted and this step is noted as “FULL CLOSED.”
  • the reflective surface 25 is omitted from FIGS. 4A-4E , but is shown on first shutter blade 26 in FIG. 4F .
  • a first open-biased reference aperture 50 in the first shutter blade 26 and a second open-biased reference aperture 52 in the second shutter blade 28 are positioned to completely overlap in the full open position; the full open position defined as complete overlap of first and second light transmitting apertures 32 and 36 , respectively, and as shown in FIG. 5A .
  • a first sensor 60 functionally referred to as a blades-open sensor and shown in FIGS. 6A-6C , is positioned on a back plate 64 supporting the shutter assembly 18 and aligned with the first and second open-biased reference apertures 50 and 52 , respectively, in the full open position.
  • first closed-biased reference aperture 56 and second closed-biased reference aperture 58 are positioned to completely overlap in the full closed position as shown in FIG. 5F .
  • a second sensor 62 functionally referred to as a blades-closed sensor and shown in FIGS. 6A-6C , is positioned on a back plate 64 supporting the shutter assembly 18 and aligned with the first and second closed-biased reference apertures 56 and 58 , respectively, in the full closed position.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Immunology (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pathology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Analytical Chemistry (AREA)
  • Hematology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Microbiology (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Medicinal Chemistry (AREA)
  • Food Science & Technology (AREA)
  • Optics & Photonics (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Shutters For Cameras (AREA)

Abstract

A shutter assembly includes a first shutter blade having a first toothed arm extending therefrom and a first light transmitting aperture therein, and a second shutter blade positioned adjacent and parallel to the first shutter blade. The second shutter blade has a second toothed arm extending therefrom and a second light transmitting aperture therein. The first and second shutter blades are supported to allow parallel linear motion. A motor gear is disposed between, and meshed with, the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
This is a continuation application of U.S. Ser. No. 14/403,381, filed Nov. 24, 2014 which claims the benefit of US National Stage of International Application No. PCT/US2013/042372, filed May 23, 2013 and claims priority under 35 U.S.C. 119(e) to U.S. Provisional Application No. 61/652,553, filed May 29, 2012. All of the applications are incorporated by reference herein in their entirety.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
Not applicable.
BACKGROUND OF THE INVENTIVE CONCEPTS 1. Field of the Inventive Concepts
The inventive concepts disclosed and claimed herein relate generally to shutters, and more particularly, but not by way of limitation, to a shutter assembly for protecting a sensitive light detector such as a photomultiplier tube against harmful exposure to light.
2. Brief Description of Related Art
Analytical instrumentation utilizing luminescence detection is heavily utilized in the pharmaceutical and medical industries. Analytical measurements are often performed using a beam of catalyzing radiation to interact with a specific sample-reagent combination. The resulting photon emission, often very weak, is then detected and measured with a sensitive detector, converted to an electrical signal, and further correlated to provide the actual analytical result.
For example, U.S. Pat. No. 5,709,994 discloses a highly sensitive method of assaying known as a Luminescent Oxygen Channeling Immunoassay (LOCI). The method uses a photosensitizer that generates singlet oxygen upon irradiation, and a chemiluminescent compound that is activated by the singlet oxygen. The photosensitizer and chemiluminescent compound are irradiated with light of a certain wavelength, after which the resulting light emitted by chemiluminescent compound is measured and correlated to provide the assay.
The instrumentation utilized for luminescence-based assays is often physically large due, in part, to the intricate and sensitive optics used. The analyses often involve exposure of the sample to a high intensity light near the field of view of a sensitive detector such as a photomultiplier tube. To protect the sensitive detector, it is common to widely separate the detector from the high intensity light source and to provide path barriers and shutters between the two.
Size is not a major concern in large laboratories facilitating high-throughput screening; however, it would be useful to have a lighter, portable unit or handheld device capable of producing accurate luminescence-based analyses for non-laboratory settings, such as, medical clinics, physicians offices and homes. Compact designs that reduce the optical path can also increase the risk of harmful exposure of the sensitive detector to the high intensity light source.
In view of the foregoing, there is an increasing need for a shutter design that is compact, energy-efficient, and suitable for protecting sensitive detectors in a portable luminescence-based sample analyzer. It is to such a shutter design that the presently disclosed and claimed inventive concept(s) is directed.
SUMMARY OF THE INVENTIVE CONCEPTS
The inventive concepts disclosed and claimed herein generally relate to a shutter assembly for interrupting light transmission. The shutter assembly includes a first shutter blade having a first toothed arm extending therefrom and a first light transmitting aperture therein, and a second shutter blade positioned adjacent and parallel to the first shutter blade. The second shutter blade has a second toothed arm extending therefrom and a second light transmitting aperture therein. The first and second shutter blades are supported to allow parallel linear motion. A motor gear is disposed between, and meshed with, the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another.
BRIEF DESCRIPTION OF THE DRAWINGS
Like reference numerals in the figures represent and refer to the same or similar element or function. Implementations of the disclosure may be better understood when consideration is given to the following detailed description thereof. Such description makes reference to the annexed pictorial illustrations, schematics, graphs, and drawings. The figures are not necessarily to scale and certain features and certain views of the figures may be shown exaggerated, to scale or in schematic in the interest of clarity and conciseness. In the drawings:
FIG. 1 is a schematic representation of an embodiment of a sample analyzer constructed in accordance with the inventive concepts disclosed herein.
FIG. 2 is a schematic representation of an embodiment of a shutter assembly constructed in accordance with the inventive concepts disclosed herein.
FIG. 3 is a timing diagram for an embodiment of a sample analyzer operation in accordance with the inventive concepts disclosed herein.
FIG. 4A-FIG. 4F provide a schematic representation of a shutter assembly embodiment operating in accordance with the inventive concepts disclosed herein.
FIG. 5A-FIG. 5F provide a schematic representation of another shutter assembly embodiment operating in accordance with the inventive concepts disclosed herein.
FIG. 6A-FIG. 6C provide a schematic representation of yet another shutter assembly embodiment showing use and placement of reference aperture sensors.
DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS
Before explaining at least one embodiment of the inventive concept disclosed herein in detail, it is to be understood that the inventive concept is not limited in its application to the details of construction, experiments, exemplary data, and/or the arrangement of the components set forth in the following description, or illustrated in the drawings. The presently disclosed and claimed inventive concept is capable of other embodiments or of being practiced or carried out in various ways. Also, it is to be understood that the phraseology and terminology employed herein is for purpose of description only and should not be regarded as limiting in any way.
In the following detailed description of embodiments of the inventive concept, numerous specific details are set forth in order to provide a more thorough understanding of the inventive concept. However, it will be apparent to one of ordinary skill in the art that the inventive concept within the disclosure may be practiced without these specific details. In other instances, well-known features have not been described in detail to avoid unnecessarily complicating the instant disclosure.
Further, unless expressly stated to the contrary, “or” refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by anyone of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
In addition, use of the “a” or “an” are employed to describe elements and components of the embodiments herein. This is done merely for convenience and to give a general sense of the inventive concept. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.
References to the Luminescent Oxygen Channeling Immunoassay (LOCI) methods and optical systems are for example only, and the inventive concepts can be used with any sample analysis procedure utilizing optical detection to measure luminescence, fluorescence, absorbance, and turbidity. Reference to a “sample” or “assay sample” refers to the sample to be analyzed and includes reagents added according to the analysis procedure, those reagents added either before or after insertion into the assay sample vessel.
Finally, as used herein any reference to “one embodiment” or “an embodiment” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. The appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
Referring now to the drawings, and more particularly to FIG. 1, shown therein is an exemplary embodiment of a sample analyzer 10 constructed in accordance with the inventive concepts disclosed and claimed herein. The sample analyzer 10 comprises an illuminator 12 for illuminating an assay sample 14 positioned and contained within a sample reservoir 16 to cause luminescence. A shutter assembly 18 is positioned along an optical axis 20 to protect the sensitive optics of detector 22 from high intensity illumination from the illuminator 12. The detector 22 measures the luminescence or light emitted from assay sample 14 as a result of the illumination.
The illuminator 12 can be multi-wavelength, optionally filtered to cut off undesired wavelengths, or can be a laser providing monochromatic light. Light intensity and time of irradiation may vary widely. In one embodiment, light emitting diodes (LEDs) are used. In another embodiment, the illuminator 12 comprises multiple LEDs arranged in a ring.
The detector 22 can be any known or yet to be developed photo-detector having a sensitivity required by the particular assay. For example, vacuum photodetectors such as photomultiplier tubes (PMTs) are typically very sensitive compared to solid state photodetectors such as silicon photodiodes. Photodetectors and their use are well known to those skilled in the art.
Optical axis 20 is defined herein by a line directed from the illuminator 12 to the detector 22. In some embodiments, and as shown in FIG. 1, optical axis 20 also coincides with a line directed from the positioned sample reservoir 16 to the detector 22. Such alignment of the illuminator 12 with both the sample reservoir 16 and the detector 22 provides a shortened optical path for both illumination and measuring modes. This in turn allows a more compact design and reduced power requirements compared to existing laboratory luminescence-based sample analyzers. For example, in one embodiment, the detector 22 is positioned about 10 mm or less from the assay sample 14. In another embodiment, the detector 22 is positioned about 5 mm or less from the assay sample 14. This is significantly more compact than present bench scale sample analyzers wherein the distance between the detector and the assay sample is on the order of 80 mm or more. Also, in one embodiment, the detector 22 is positioned about 5 mm from the illuminator 12. This is a significant achievement, particularly in embodiments utilizing a photomultiplier tube to measure extraordinarily low light signals of interest on the order of 50 photons per second output. Such compaction provides embodiments wherein the sample analyzer 10 is portable and/or hand-held and the power supply 24 is one or more batteries.
The shutter assembly 18 operates to remain closed during the illumination interval, thereby blocking light transmission from the illuminator 12 to the detector 22 and protecting the detector 22 from over exposure. During the illumination interval, light shines into the assay sample reservoir 16, activating the assay sample 14 to start the reaction and photon emission. After the illumination interval, the assay sample 14 begins to respond by emitting photons and during this measuring mode, the shutter assembly 18 remains open to allow light emitted by the assay sample to enter and be measured by detector 22. This unique design enables the use of rigid, dense blade material, such as metal alloys, achieving the highest degree of optical density performance possible while providing high speed shutter opening and closing, a critical need in high intensity illumination applications that use a high sensitivity photon detector.
In one embodiment, a surface 25 of the shutter assembly 18 facing the illuminator 12 is reflective, such that light from the illuminator 12 passing through the assay sample 14 is reflected by the surface 25 back toward the assay sample 14. This increases the illumination penetrating the assay sample 14 and thereby improves the assay sample activation. A nonlimiting example of a suitable reflective surface 25 is polished stainless steel.
As shown in FIG. 2, the shutter assembly 18 comprises a first shutter blade 26 and a second shutter blade 28. First shutter blade 26 is planar in shape with a first toothed arm 30 extending therefrom and a first light transmitting aperture 32 therein. Similarly, the second shutter blade 28 is planar in shape with a second toothed arm 34 extending therefrom and a second light transmitting aperture 36 therein. The second shutter blade 28 is positioned adjacent and parallel to the first shutter blade 26, and both shutter blades 26 and 28 are slideably supported on shutter assembly 18 to allow parallel linear motion.
First and second shutter blades 26 and 28 are typically shaped as thin metal blades with dimensions determined, in large part, by the sizes of the sample reservoir 16 and detector 22. Suitable construction can include any rigid material that is impervious to light. A variety of suitable metal alloys and polymers are known to those skilled in the art and are readily available commercially.
In one prototype, the first and second shutter blades 26 and 28 were constructed of 0.127 mm thick 304 stainless steel. This material is readily available and provided a high degree of light blocking. The blades were treated with a black oxide coating to prevent photon tunneling and reflections. The friction caused between the blades was low, thereby providing a low torque requirement and allowing high speed operation.
The reflective surface 25 can be present on at least a portion of the first or second shutter blades 26 and 28, wherein that portion represents the shutter blade surface exposed to illumination penetrating through the assay sample 14 during the illumination interval. It has been found that when first and second shutter blades 26 and 28 are constructed of stainless steel, polishing a portion of the stainless steel to produce the reflective surface 25 is sufficient to increase the illumination penetrating the assay sample 14 and to improve the assay sample activation. First shutter blade 26 can include a lower arm 54 which does not require teeth as do first and second toothed arms 30 and 34.
The shutter assembly 18 is operated by an actuator mechanism to cause the first and second shutter blades 26 and 28, respectively, to move linearly in opposite directions between an open position in which the first and second light transmitting apertures 32 and 36 are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures 32 and 36 are in a non-overlapping relationship with respect to one another. Non-limiting examples of a suitable shutter actuator mechanism include a motor and solenoid with linkage to the shutter working against a spring, and a stepper motor.
A spring (not shown) or the like may be used to urge the first and second shutter blades 26 and 28 into a closed position to protect the detector 22. Shutters, such as those used in cameras and laboratory instrumentation utilizing optical detection, such as luminescence, fluorescence, absorbance measurements, are commonly controlled using a solenoid working against a spring. The solenoid requires continued power input to work against the spring or the like to maintain the shutter in an open position. The analytical instruments requiring shutters are usually powered by AC current, and the solenoid power requirements are not a major concern. Battery power drain is not significant with camera shutters because the shutter typically does not remain open for long periods. However, because of the relatively long time the shutter must remain open in luminescence-based sample analyzers, the power required for operation of a solenoid-controlled shutter in a battery-operated luminescence-based sample analyzer is significant.
In one embodiment, a motor 38, attached to the shutter assembly 18 by, for example, mountings 40 a and 40 b, provides a gear 42 which is disposed between, and meshed with, the first and second toothed arms 30 and 34, respectively. Rotation of gear 42 causes the first and second shutter blades 26 and 28, respectively, to move linearly in opposite directions between an open position in which the first and second light transmitting apertures 32 and 36 are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures 32 and 36 are in a non-overlapping relationship with respect to one another.
In one embodiment, motor 38 is a stepper motor. A stepper motor is a brushless, electric motor having a number of “toothed” electromagnets arranged around a central gear-shaped bar of iron, each electromagnet providing a “step.” A full rotation is thus divided into a number of individual steps, and the motor's position can be precisely controlled without requiring a feedback mechanism. As the speed of the stepper motor increases, torque decreases. The maximum torque occurs when the motor is stationary, and this “holding torque” determines the ability of the motor to maintain a desired position under external load. Thus, stepper motor 38 advantageously provides a holding torque which can be used to maintain the shutter blades in a precisely controlled position, whether closed, full open, or any position between. Because the stepper motor 38 requires no power to maintain a shutter position, it reduces the power requirements of a portable luminescence-based analyzer making such battery powered devices practical.
Additionally, the time taken for stepper motor 38 to open first and second shutter blades 26 and 28, respectively, is fast, due in part because the mass of the shutter blades and resulting inertia is small, and because the stepper motor 38 can be run at its highest velocity, sometimes called “high speed slewing.” Thus, the shutter assembly 18 utilizing stepper motor 38 can be used to control the exposure time of the detector 22 in addition to protecting the detector 22 from light from the illuminator 12.
In a typical LOCI assay method such as for Troponin I, a patient blood plasma sample is mixed with chemi-bead and biotinylated antibody reagents and incubated at 37° C. for a specified time. This sample reagent mixture is then added to the sensi-bead reagent and incubated at 37° C. for a specified time. This mixture is diluted with assay diluent resulting in a assay sample which is illuminated with 680 nm light. This causes singlet oxygen release and shortly afterward emission of 612 nm photons which are measured by an optical detection system. FIG. 3 is an example timing diagram depicting a LOCI Troponin I assay. Process timing is shown for the illumination step, operation of photomultiplier shutter assembly and signal gates, and the production and analysis of photons emitted from the catalyst in the assay sample. FIG. 3 timing sequence detail: First the assay sample is illuminated; Second the shutter is opened to expose the detector optics to the assay sample; Third the detector is logically enabled to collect photon emission; Fourth the detector collecting photon emission is logically disabled; Fifth the shutter is closed to occlude and protect the detector. The Notional Assay Flux Production waveform represents the signal of interest, the output of the assay sample is proportional to the analyte concentration.
Referring now to FIG. 4A, the first and second shutter blades 26 and 28 are noted at stepper motor 38 position “0” coinciding with the first and second light transmitting apertures 32 and 36, respectively, being fully aligned thereby providing a full effective aperture 44 and noted as “FULL OPEN.” FIG. 4B through FIG. 4F show an example of the relative positions of the shutter blades and apertures as stepper motor gear 42 progresses in 2-step intervals. After 6 steps, FIG. 4D shows no overlap of the first and second light transmitting apertures 32 and 36, respectively, and therefore no effective aperture 44.
In one embodiment, reference apertures are also provided in the shutter blades. For example, FIG. 4A through FIG. 4F show the relative positions of a pinhole reference aperture 46 in the first shutter blade 26, and a larger reference aperture 48 in the second shutter blade 28. In one embodiment, the pinhole reference aperture 46 has a diameter of about 0.5 mm or less. In another embodiment, the larger reference aperture 48 has a diameter less than 25 percent of the diameter of the first and second light transmitting apertures 32 and 36. The pinhole reference aperture 46 and the large reference aperture 48 are positioned on either side of the respective first or second light transmitting aperture 26 or 28, such that they are at a maximum distance of separation in the full open position shown in FIG. 4A, and overlapping after 8 steps as shown in FIG. 4E. The pinhole reference aperture, positioned as in FIG. 4E, allows only small quantities of light into the detector 22, and can be used to monitor alignment or the light intensity transmitted by illuminator 12 for example. In FIG. 4F, no light may be transmitted and this step is noted as “FULL CLOSED.” The reflective surface 25 is omitted from FIGS. 4A-4E, but is shown on first shutter blade 26 in FIG. 4F.
In another embodiment, and as shown schematically in FIG. 5A through 5E, a first open-biased reference aperture 50 in the first shutter blade 26 and a second open-biased reference aperture 52 in the second shutter blade 28 are positioned to completely overlap in the full open position; the full open position defined as complete overlap of first and second light transmitting apertures 32 and 36, respectively, and as shown in FIG. 5A. A first sensor 60, functionally referred to as a blades-open sensor and shown in FIGS. 6A-6C, is positioned on a back plate 64 supporting the shutter assembly 18 and aligned with the first and second open-biased reference apertures 50 and 52, respectively, in the full open position. Similarly, first closed-biased reference aperture 56 and second closed-biased reference aperture 58 are positioned to completely overlap in the full closed position as shown in FIG. 5F. A second sensor 62, functionally referred to as a blades-closed sensor and shown in FIGS. 6A-6C, is positioned on a back plate 64 supporting the shutter assembly 18 and aligned with the first and second closed-biased reference apertures 56 and 58, respectively, in the full closed position.
From the above description, it is clear that the inventive concept(s) disclosed herein is well adapted to carry out the objects and to attain the advantages mentioned herein as well as those inherent in the inventive concept disclosed herein. While exemplary embodiments of the inventive concept disclosed herein have been described for purposes of this disclosure, it will be understood that numerous changes may be made which will readily suggest themselves to those skilled in the art and which are accomplished without departing from the scope of the inventive concept disclosed herein and defined by the appended claims.

Claims (28)

What is claimed is:
1. A shutter assembly, comprising:
an illuminator;
a shutter assembly comprising a first shutter blade, a second shutter blade, and a motor;
the first shutter blade having a first toothed arm extending therefrom and a first light transmitting aperture therein;
the second shutter blade positioned adjacent and parallel to the first shutter blade, the second shutter blade having a second toothed arm extending therefrom and a second light transmitting aperture therein, the first and second shutter blades supported to allow parallel linear motion; and
a motor having a gear disposed between, and meshed with, the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another along the optical axis, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another; and
wherein the shutter assembly and the assay are positioned along an optical axis extending from the illuminator, through the assay sample and the first and second light transmitting apertures of the shutter assembly when the first and second shutter blades are in the open position.
2. The shutter assembly of claim 1, wherein the motor and gear provide a direct drive mechanism.
3. The shutter assembly of claim 1, wherein the motor is a stepper motor.
4. The shutter assembly of claim 1, wherein the motor is a battery-powered stepper motor.
5. The shutter assembly of claim 1, wherein at least a portion of one of the first and second shutter blades has a polished reflective surface.
6. The shutter assembly of claim 1, further comprising a first reference aperture in the first shutter blade positioned to align with the second light transmitting aperture in the second blade prior to alignment of the first and second light transmitting apertures in the open position.
7. The shutter assembly of claim 6, wherein the first reference aperture is positioned along a center line connecting the first light transmitting aperture and the second light transmitting aperture, such that overlap of the first reference aperture with the second light transmitting aperture provides a trace of the movement of the first and second shutter blades between the closed position and the open position.
8. The shutter assembly of claim 6, wherein the reference aperture has a diameter less than 25 percent of the diameter of the first and second light transmitting apertures.
9. The shutter assembly of claim 6, wherein the reference aperture is a pinhole having a diameter of 0.5 mm or less.
10. The shutter assembly of claim 6, further comprising a second reference aperture in the second shutter blade positioned along the center line.
11. The shutter assembly of claim 1, further comprising a first open-biased reference aperture in the first shutter blade and a second open-biased reference aperture in the second shutter blade, the first and second open-biased reference apertures positioned such that they overlap only at the open position.
12. The shutter assembly of claim 11, wherein the first and second open-biased reference apertures have a diameter less than 25 percent of the diameter of the first and second light transmitting apertures.
13. The shutter assembly of claim 11, further comprising a first sensor positioned adjacent the first and second open-biased reference apertures in the overlapping position, so as to confirm that the first and second shutter blades are in the open position.
14. The shutter assembly of claim 1, further comprising a first closed-biased reference aperture in the first shutter blade and a second closed-biased reference aperture in the second shutter blade, the first and second closed-biased reference apertures positioned such that they overlap only at the closed position.
15. The shutter assembly of claim 14, wherein the first and second closed-biased reference apertures have a diameter less than 25 percent of the diameter of the first and second light transmitting apertures.
16. The shutter assembly of claim 14, further comprising a second sensor positioned adjacent the first and second open-biased reference apertures in the overlapping position, so as to confirm that the first and second shutter blades are in the open position.
17. A sample analyzer, comprising:
an illuminator;
such that the illuminator causes luminescence or fluorescence of the assay sample;
a detector positioned along an optical axis extending from the illuminator, through the assay sample, to the detector, so as to detect the luminescence or fluorescence of the assay sample; and
a shutter assembly positioned along the optical axis and adjacent the detector, operable to interrupt light from the illuminator, the shutter assembly having:
a first shutter blade with a first toothed arm extending therefrom and a first light transmitting aperture therein;
a second shutter blade positioned adjacent and parallel to the first shutter blade, the second shutter blade having a second toothed arm extending therefrom and a second light transmitting aperture therein, the first and second shutter blades supported to allow parallel linear motion; and
a motor having a gear disposed between and meshed with the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another
wherein the assay sample is disposed in between the illuminator and the shutter assembly along the optical axis
wherein the apparatus is configured with an illumination mode and a measurement mode,
wherein during the illumination mode the motor moves the first and second shutter blades to the closed position and the illuminator is operated to illuminate the assay sample;
wherein during the measurement mode the illuminator is operated to discontinue illuminating the sample;
further wherein during the measurement mode the motor moves the first and second shutter blades to the open position such that luminescence from the assay sample passes through the first and second light transmitting apertures to the detector along the optical axis.
18. The sample analyzer of claim 17, wherein the detector is a photomultiplier tube.
19. The sample analyzer of claim 17, wherein the detector is positioned less than 10 mm from the assay sample.
20. The sample analyzer of claim 17, wherein the detector is positioned 5 mm to 15 mm from the illuminator.
21. The sample analyzer of claim 17, wherein a reflective surface is provided on at least a portion of the first or second shutter blades, wherein that portion represents a shutter blade surface adjacent the assay sample when the first and second light transmitting apertures are in the closed position.
22. A method of analyzing as assay sample, comprising:
obtaining a sample analyzer comprising:
an illuminator;
a detector positioned along an optical axis extending from the illuminator, through the assay sample, to the detector; and
a shutter assembly, positioned along the optical axis and adjacent the detector, the shutter assembly comprising:
a first shutter blade having a first toothed arm extending therefrom and a first light transmitting aperture therein;
a second shutter blade positioned adjacent and parallel to the first shutter blade, the second shutter blade having a second toothed arm extending therefrom and a second light transmitting aperture therein, the first and second shutter blades supported to allow parallel linear motion; and
a motor having a gear disposed between, and meshed with, the first and second toothed arms such that rotation of the gear causes the first and second shutter blades to move linearly in opposite directions between an open position in which the first and second light transmitting apertures are in an overlapping relationship with respect to one another, and a closed position in which the first and second light transmitting apertures are in a non-overlapping relationship with respect to one another
wherein the assay sample is disposed in between the illuminator and the shutter assembly along the optical axis;
supporting the sample vessel containing the assay sample proximate to the illuminator;
illuminating the assay sample to cause luminescence of the assay sample during an illumination mode of the sample analyzer;
operating the shutter assembly to cause the first and second shutter blades to reach and maintain a closed position during the illumination mode;
discontinuing the illumination of the sample during a measurement mode of the sample analyzer;
operating the shutter assembly to cause the first and second shutter blades to reach and maintain an open position during the measurement mode such that luminescence from the assay sample passes through the first and second light transmitting apertures towards the detector along the optical axis; and
measuring the luminescence or fluorescence.
23. The method of claim 22, wherein the motor and gear provide a direct drive mechanism.
24. The method of claim 22, wherein the motor is a stepper motor.
25. The method of claim 22, wherein a reflective surface is provided on at least a portion of the first or second shutter blades, wherein that portion represents a shutter blade surface adjacent the assay sample when the first and second light transmitting apertures are in the closed position.
26. The method of claim 22, wherein the motor is a battery-powered stepper motor.
27. The method of claim 22, wherein the motor has a single gear disposed between and meshed with, the first and second toothed arms.
28. The method of claim 22, wherein the shutter assembly further comprises a first reference aperture in the first shutter blade, positioned to align with the second light transmitting aperture in the second blade prior to alignment of the first and second light transmitting apertures in the open position.
US15/691,842 2012-05-29 2017-08-31 Shutter assembly for a luminescence-based sample analyzer Active US10078215B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/691,842 US10078215B2 (en) 2012-05-29 2017-08-31 Shutter assembly for a luminescence-based sample analyzer

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201261652553P 2012-05-29 2012-05-29
PCT/US2013/042372 WO2013181052A1 (en) 2012-05-29 2013-05-23 Shutter assembly for a luminescence-based sample analyzer
US201414403381A 2014-11-24 2014-11-24
US15/691,842 US10078215B2 (en) 2012-05-29 2017-08-31 Shutter assembly for a luminescence-based sample analyzer

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2013/042372 Continuation WO2013181052A1 (en) 2012-05-29 2013-05-23 Shutter assembly for a luminescence-based sample analyzer
US14/403,381 Continuation US9791690B2 (en) 2012-05-29 2013-05-23 Shutter assembly for a luminescence-based sample analyzer

Publications (2)

Publication Number Publication Date
US20180045950A1 US20180045950A1 (en) 2018-02-15
US10078215B2 true US10078215B2 (en) 2018-09-18

Family

ID=49673830

Family Applications (2)

Application Number Title Priority Date Filing Date
US14/403,381 Active US9791690B2 (en) 2012-05-29 2013-05-23 Shutter assembly for a luminescence-based sample analyzer
US15/691,842 Active US10078215B2 (en) 2012-05-29 2017-08-31 Shutter assembly for a luminescence-based sample analyzer

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US14/403,381 Active US9791690B2 (en) 2012-05-29 2013-05-23 Shutter assembly for a luminescence-based sample analyzer

Country Status (12)

Country Link
US (2) US9791690B2 (en)
EP (1) EP2856254B1 (en)
JP (2) JP2015525372A (en)
KR (1) KR20150016384A (en)
CN (1) CN104321698B (en)
BR (1) BR112014029494A2 (en)
CA (1) CA2875126A1 (en)
DK (1) DK2856254T3 (en)
ES (1) ES2768401T3 (en)
IN (1) IN2014DN08674A (en)
MX (1) MX346207B (en)
WO (1) WO2013181052A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2976619B1 (en) 2013-03-20 2021-11-10 Siemens Healthcare Diagnostics Inc. Light and shutter for a sample analyzer
EP3685131B1 (en) 2017-09-19 2022-09-07 Beckman Coulter, Inc. Analog light measuring and photon counting in chemiluminescence measurements
FR3082224B1 (en) * 2018-06-07 2020-05-22 Openfield MINI-TURBINE FLOWMETER AND DOWNHOLE TOOL COMPRISING A MINI-TURBINE FLOWMETER ARRAY FOR OPERATING IN A HYDROCARBON WELL.
CN109738403A (en) * 2019-01-03 2019-05-10 必欧瀚生物技术(合肥)有限公司 A kind of preparation method of fluorescence standard card and fluorescence standard card fluorescent film
CN110625257B (en) * 2019-09-26 2021-09-28 中国科学院重庆绿色智能技术研究院 Vacuum-resistant evaporation plating metal additive manufacturing device and working and manufacturing method thereof

Citations (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB456617A (en)
US2922349A (en) 1955-08-08 1960-01-26 Seton I Rochwite Stereoscopic camera
JPS5011432A (en) 1973-05-22 1975-02-05
US3903528A (en) 1973-05-22 1975-09-02 Polaroid Corp Exposure control system for photographic apparatus
US3918077A (en) 1974-05-06 1975-11-04 Terminal Data Corp Translational shutter system
US3928859A (en) 1974-03-22 1975-12-23 Honeywell Inc Shutter-iris for automatic camera
JPS5158329A (en) 1974-11-18 1976-05-21 Fuji Photo Film Co Ltd
US4007469A (en) 1975-04-21 1977-02-08 Polaroid Corporation Photographic apparatus with plurality of selectively determinable operational modes
JPS52117124A (en) 1976-03-26 1977-10-01 Fuji Photo Film Co Ltd Two-blade shutter
US4112450A (en) 1976-02-18 1978-09-05 Fuji Photo Film Co., Ltd. Shutter device for a photographic camera
JPS548523A (en) 1977-06-21 1979-01-22 Canon Inc Exposure controller of cameras
US4176929A (en) 1977-06-21 1979-12-04 Canon Kabushiki Kaisha Exposure control device for a camera
JPS60249123A (en) 1984-05-25 1985-12-09 Canon Inc Pulse driving shutter
US4827348A (en) 1988-05-02 1989-05-02 Polaroid Corporation Exposure control system for dual mode electronic imaging camera
JPH01257927A (en) 1988-04-08 1989-10-16 Seikosha Co Ltd Motor driving device
US4978991A (en) 1989-12-29 1990-12-18 Polaroid Corporation Open-loop stepper motor controlled shutter
JPH0590457U (en) 1991-06-26 1993-12-10 ニスカ株式会社 Light intensity adjustment device
JPH0643090A (en) 1992-04-01 1994-02-18 Toa Medical Electronics Co Ltd Particle analyzer
US5408363A (en) 1991-06-21 1995-04-18 Kano; Tetsuhiro Reflector and a method of generating a reflector shape
US5709994A (en) 1992-07-31 1998-01-20 Syntex (U.S.A.) Inc. Photoactivatable chemiluminescent matrices
US5833924A (en) 1995-12-22 1998-11-10 Universal Healthwatch, Inc. Sampling-assay device and interface system
US6139153A (en) 1996-03-04 2000-10-31 Arnold & Richter Cine Technik Gmbh & Co. Betreibs Kg Motion picture camera with a capping shutter
US6313471B1 (en) 1998-08-18 2001-11-06 Molecular Devices Corporation Scanning fluorometer
US6466353B2 (en) 1998-03-06 2002-10-15 Electro-Optical Products Corp. Low frequency optical shutter and driver
US6495373B1 (en) 1998-10-14 2002-12-17 Polaroid Corporation Method and apparatus for performing diagnostic tests
JP2004348051A (en) 2003-05-26 2004-12-09 Alps Electric Co Ltd Shutter driving device in common use as diaphragm
US6850351B1 (en) 2003-02-20 2005-02-01 Team Specialty Products Corp. Method and apparatus for ultra-fast aperture exposure
CN1664689A (en) 2004-03-05 2005-09-07 尼司卡股份有限公司 Imaging apparatus and light quantity regulating device used therein
JP2007156230A (en) 2005-12-07 2007-06-21 Seiko Epson Corp Optical diaphragm device and projector
US20070177049A1 (en) 2006-01-30 2007-08-02 Radiant Imaging, Inc. Rotary shutter assemblies for imaging photometers and methods for using such shutter assemblies
US20080129736A1 (en) 2006-11-30 2008-06-05 Fluidigm Corporation Method and apparatus for biological sample analysis
US7402281B2 (en) 2003-07-18 2008-07-22 Siemens Healthcare Diagnostics Inc. Magazine for inventorying reaction cuvettes in an automatic analyzer
CN101266386A (en) 2007-03-15 2008-09-17 上海乐金广电电子有限公司 Miniature camera aperture shutter device
WO2009111834A1 (en) 2008-03-14 2009-09-17 Runcie John W Automated shutter for dark acclimating samples
US20100024526A1 (en) 2008-07-28 2010-02-04 Sensors For Medicine & Science, Inc. Systems and methods for optical measurement of analyte concentration
US20100276605A1 (en) 2007-10-04 2010-11-04 Danmarks Tekniske Universitet Detector for detecting particle radiation of an energy in the range of 150 ev to 300 kev, and a materials mapping apparatus with such a detector
US20110007312A1 (en) 2009-07-08 2011-01-13 Battelle Memorial Institute System and method for high precision isotope ratio destructive analysis
US20120231493A1 (en) 2007-04-20 2012-09-13 Hideyuki Noda Apparatus for chemiluminescent assay and detection
EP3325410A1 (en) 2015-07-21 2018-05-30 Sharp Kabushiki Kaisha Layered oxide materials for batteries

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2214648A (en) 1988-01-19 1989-09-06 Photo Me Int An identity-portrait camera

Patent Citations (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB456617A (en)
US2922349A (en) 1955-08-08 1960-01-26 Seton I Rochwite Stereoscopic camera
JPS5011432A (en) 1973-05-22 1975-02-05
US3903528A (en) 1973-05-22 1975-09-02 Polaroid Corp Exposure control system for photographic apparatus
GB1474038A (en) 1973-05-22 1977-05-18 Polaroid Corp Photographic exposure control mechanism
US3928859A (en) 1974-03-22 1975-12-23 Honeywell Inc Shutter-iris for automatic camera
US3918077A (en) 1974-05-06 1975-11-04 Terminal Data Corp Translational shutter system
JPS5158329A (en) 1974-11-18 1976-05-21 Fuji Photo Film Co Ltd
US4007469A (en) 1975-04-21 1977-02-08 Polaroid Corporation Photographic apparatus with plurality of selectively determinable operational modes
US4112450A (en) 1976-02-18 1978-09-05 Fuji Photo Film Co., Ltd. Shutter device for a photographic camera
JPS52117124A (en) 1976-03-26 1977-10-01 Fuji Photo Film Co Ltd Two-blade shutter
JPS548523A (en) 1977-06-21 1979-01-22 Canon Inc Exposure controller of cameras
US4176929A (en) 1977-06-21 1979-12-04 Canon Kabushiki Kaisha Exposure control device for a camera
JPS60249123A (en) 1984-05-25 1985-12-09 Canon Inc Pulse driving shutter
JPH01257927A (en) 1988-04-08 1989-10-16 Seikosha Co Ltd Motor driving device
US4827348A (en) 1988-05-02 1989-05-02 Polaroid Corporation Exposure control system for dual mode electronic imaging camera
US4978991A (en) 1989-12-29 1990-12-18 Polaroid Corporation Open-loop stepper motor controlled shutter
US5408363A (en) 1991-06-21 1995-04-18 Kano; Tetsuhiro Reflector and a method of generating a reflector shape
JPH0590457U (en) 1991-06-26 1993-12-10 ニスカ株式会社 Light intensity adjustment device
JPH0643090A (en) 1992-04-01 1994-02-18 Toa Medical Electronics Co Ltd Particle analyzer
US5709994A (en) 1992-07-31 1998-01-20 Syntex (U.S.A.) Inc. Photoactivatable chemiluminescent matrices
US5833924A (en) 1995-12-22 1998-11-10 Universal Healthwatch, Inc. Sampling-assay device and interface system
US6139153A (en) 1996-03-04 2000-10-31 Arnold & Richter Cine Technik Gmbh & Co. Betreibs Kg Motion picture camera with a capping shutter
US6466353B2 (en) 1998-03-06 2002-10-15 Electro-Optical Products Corp. Low frequency optical shutter and driver
US6313471B1 (en) 1998-08-18 2001-11-06 Molecular Devices Corporation Scanning fluorometer
US6495373B1 (en) 1998-10-14 2002-12-17 Polaroid Corporation Method and apparatus for performing diagnostic tests
US6850351B1 (en) 2003-02-20 2005-02-01 Team Specialty Products Corp. Method and apparatus for ultra-fast aperture exposure
JP2004348051A (en) 2003-05-26 2004-12-09 Alps Electric Co Ltd Shutter driving device in common use as diaphragm
US7402281B2 (en) 2003-07-18 2008-07-22 Siemens Healthcare Diagnostics Inc. Magazine for inventorying reaction cuvettes in an automatic analyzer
CN1664689A (en) 2004-03-05 2005-09-07 尼司卡股份有限公司 Imaging apparatus and light quantity regulating device used therein
JP2007156230A (en) 2005-12-07 2007-06-21 Seiko Epson Corp Optical diaphragm device and projector
US20070177049A1 (en) 2006-01-30 2007-08-02 Radiant Imaging, Inc. Rotary shutter assemblies for imaging photometers and methods for using such shutter assemblies
US20080129736A1 (en) 2006-11-30 2008-06-05 Fluidigm Corporation Method and apparatus for biological sample analysis
CN101266386A (en) 2007-03-15 2008-09-17 上海乐金广电电子有限公司 Miniature camera aperture shutter device
US20120231493A1 (en) 2007-04-20 2012-09-13 Hideyuki Noda Apparatus for chemiluminescent assay and detection
US20100276605A1 (en) 2007-10-04 2010-11-04 Danmarks Tekniske Universitet Detector for detecting particle radiation of an energy in the range of 150 ev to 300 kev, and a materials mapping apparatus with such a detector
WO2009111834A1 (en) 2008-03-14 2009-09-17 Runcie John W Automated shutter for dark acclimating samples
US20100024526A1 (en) 2008-07-28 2010-02-04 Sensors For Medicine & Science, Inc. Systems and methods for optical measurement of analyte concentration
US20110007312A1 (en) 2009-07-08 2011-01-13 Battelle Memorial Institute System and method for high precision isotope ratio destructive analysis
EP3325410A1 (en) 2015-07-21 2018-05-30 Sharp Kabushiki Kaisha Layered oxide materials for batteries

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
International Search Report and Written Opinion of International Application No. PCT/US2013/042372 dated Oct. 2, 2013.
Supplemental Partial European Search Report of European Application No. 13798044 dated Apr. 1, 2016.

Also Published As

Publication number Publication date
US20150097124A1 (en) 2015-04-09
US9791690B2 (en) 2017-10-17
IN2014DN08674A (en) 2015-05-22
BR112014029494A2 (en) 2017-06-27
US20180045950A1 (en) 2018-02-15
MX346207B (en) 2017-03-09
DK2856254T3 (en) 2020-02-17
JP2015525372A (en) 2015-09-03
EP2856254A1 (en) 2015-04-08
JP6494688B2 (en) 2019-04-03
EP2856254A4 (en) 2016-08-17
KR20150016384A (en) 2015-02-11
MX2014014439A (en) 2015-02-04
CN104321698B (en) 2018-02-16
WO2013181052A1 (en) 2013-12-05
EP2856254B1 (en) 2019-11-06
ES2768401T3 (en) 2020-06-22
CA2875126A1 (en) 2013-12-05
CN104321698A (en) 2015-01-28
JP2017161929A (en) 2017-09-14

Similar Documents

Publication Publication Date Title
US10078215B2 (en) Shutter assembly for a luminescence-based sample analyzer
JP2008064590A (en) Microchip inspection device
EP2466292B1 (en) System for performing scattering and absorbance assays
US9606067B2 (en) Biological assay sample analyzer
US9863879B2 (en) Light and shutter for a sample analyzer
US20150177118A1 (en) Fluidic optical cartridge
EP2893320B1 (en) Clam-shell luminometer
JP2009517653A (en) Biochip device with sample compartment and photosensitive element, method for detecting fluorescent particles in at least one sample compartment of a biochip device
WO2021038515A1 (en) Spectrofluorometric apparatus and methods for the detection of bacteria
CN111413327A (en) Dual mode detection system and dual mode detection method
KR20170032951A (en) Antigen-Antibody Detector and Antigen-Antibody Detecting Method Using Ultra-Violet Light Emitting Diode and Fluorescent Particles

Legal Events

Date Code Title Description
AS Assignment

Owner name: SIEMENS HEALTHCARE DIAGNOSTICS INC., NEW YORK

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:JASPERSE, JEFFREY R.;REEL/FRAME:043458/0394

Effective date: 20141016

FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 4